AU4147800A - Composition for preventing or treating dementia comprising hydroxycinnamic acid derivative or an extract of a plant of genus (angelicae) containing same - Google Patents

Abstract

A composition for preventing or treating dementia comprising a hydroxycinnamic acid derivative of formula (I), decursinol, a pharmaceutically acceptable salt thereof or an extract of a plant of genus Angelicae containing same, wherein, R<SUP>1 </SUP>is H or CH<SUB>3</SUB>, R<SUP>2 </SUP>is -CH-CHCOOH or formula (a).

Description

WO 00/61131 PCT/KRO0/00337 1 COMPOSITION FOR PREVENTING OR TREATING DEMENTIA COMPRISING A HYDROXYCINNAMIC ACID DERIVATIVE OR AN EXTRACT OF A PLANT OF GENUS ANGELICAE CONTAINING SAME 5 FIELD OF THE INVENTION The present invention relates to a composition for preventing or treating dementia comprising a hydroxycinnamic 10 acid derivative of formula I, decursinol, a pharmaceutically acceptable salt thereof or an extract of a plant of genus Angelicae containing same: R 2 15 (1) OR OH wherein, 20 R1 is H or CH 3 , H -0H

R

2 is -CH=CHCOOH or -CH=CHCOO-C C . C C C HO COOH 25 BACKGROUND OF THE INVENTION In recent years, an ever-increasing number of aged 30 people have become afflicted by senile dementia, e.g., Alzheimer's disease. It has been reported that accumulation of amyloid(A 4 2 ) in the brain generates neurotoxicity, which constitutes one of the causes of Alzheimer's disease(Selkoe, 35 Annu. Rev. Neurosci., 17, 489-517(1994)). Accordingly, numerous efforts have been made to develop a medicine for WO 00/61131 PCTIKR0O/00337 2 preventing or treating Alzheimer's disease by way of shielding brain cells from the toxicity of P-amyloid. However, no effective medicine has been developed. The present inventors have endeavored to develop a 5 medicine for dementia and unexpectedly found that an extract of Angelicae gigas Nakai, which has been used in Korea for treating diseases of the heart, liver and spleen, has high activity in preventing or treating dementia. 10 SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a pharmaceutical composition for preventing or treating dementia. 15 It is a further object of the present invention to provide a food composition for preventing or treating dementia. In accordance with one aspect of the present invention, there is provided a pharmaceutical composition for 20 preventing or treating dementia comprising a hydroxycinnamic acid derivative of formula I, decursinol, a pharmaceutically acceptable salt thereof or an extract of a plant of genus Angelicae containing same:

R

2 25 OR) OH 30 wherein, R1 is H or CH 3 , H1 ~OH H\C .11H

R

2 is -CH=CHCOOH or -CH=CHCoO-C C.

I I oH C C 35 \C HO~ -- \COOH WO 00/61131 PCT/KROO/00337 3 BRIEF DESCRIPTION OF THE DRAWINGS The above and other objects and features of the present invention will become apparent from the following 5 description of the invention, when taken in conjunction with the accompanying drawings, which respectively show: Figs. 1A and 1B: HPLC chromatograms confirming the presence of decursinol and ferulic acid in an extract of Angelicae gigas Nakai. 10 Fig. 2: the results of passive avoidance tests conducted employing mice administered with an extract of Angelicae gigas Nakai by changing the amount of the extract(Fig. 2A) and the period of administration(Fig. 22); Fig. 3: the results of passive avoidance tests 15 conducted employing mice administered with ferulic acid by changing the amount of ferulic acid(Fig. 3A) and the period of administration(Fig. 32); Figs. 4A and 4B: the alternation behavior(%) and the number or arm entries, respectively, observed in Y-maze 20 tests employing mice administered with ferulic acid by changing the period of administration; Fig. 5: the results of passive avoidance tests conducted employing mice administered with ferulic acid or isoferulic acid; 25 Figs. 6a to 6c: the results of passive avoidance tests, the alternation behavior(%) and the number or arm entries observed in Y-maze tests conducted employing mice administered with various amounts of decursinol, respectively; 30 Figs. 7a and 7b: synergism between ferulic acid and decursinol observed in passive avoidance tests conducted employing mice administered with ferulic acid and decursinol; Figs. 8a to 8f: micrographs of immunohistochemical 35 staining of OX-42 in pyriform cortex and amygdaloid nucleus of a mouse, taken 1 day after the administration of P- WO 00/61131 PCT/KROO/00337 4 amyloid(1-42); Figs. 9a to 9c: micrographs of immunohistochemical staining of choline acetyltransferase(ChAT) in septal nucleus of a mouse, taken 5 days after the administration of 5 P-amyloid (1-42) ; Fig. 10: the inhibitory effect of ferulic acid on amyloid(1-42) -induced leakage of lactate dehydrogenase(LDH) from the primary mouse cortical culture. 10 DETAILED DESCRIPTION OF THE INVENTION The present invention provides a pharmaceutical composition for preventing or treating dementia comprising a hydroxycinnamic acid derivative of formula I or a 15 pharmaceutically acceptable salt thereof: R(2 20 OR OH wherein, R1 is H or CH 3 , 25 H _OH CH R2 is -CH=CHCOOH or -CH=CHCOO-C C I I \OH C C C HO- COOH 30 Exemplary hydroxycinnamic acid derivative of formula I includes ferulic acid, isoferulic acid, chlorogenic acid and caffeic acid. The present invention further provides a pharmaceutical composition for preventing or treating 35 dementia comprising decursinol or a pharmaceutically acceptable salt thereof.

WO 00/61131 PCT/KROO/00337 5 The ferulic acid and decursinol can be isolated from a plant of genus Angelicae according to the method described in "Methods in New Drugs Development from Traditional Medicinal Materials" (published by Seoul National University 5 Natural Products Research Institute, Korea) , or synthesized according to the method described in Merck Index. Further, ferulic acid is commercially available and other hydroxycinnamic acid derivatives can be prepared from ferulic acid by a simple process known in the art. In 10 addition, they can be converted into various types of pharmaceutically acceptable salts, e.g., inorganic salts such as sodium, potassium, magnesium and calcium salts, and organic salts derived using angelic acid, lysine, ethanolamine, N, N' -dibenzylethylenediamine or a-tocopherol, 15 or esters ("oryzanol") derived using triterpene alcohol or plant sterols, e.g., cycloartenol, in accordance with the conventional methods well known in the art. Further, the present invention also provides a pharmaceutical composition for preventing or treating 20 dementia comprising an extract of a plant of genus Angelicae comprising the hydroxycinnamic acid derivative of formula I or decursinol. Examples of the plant of genus Angelicae useful in the present invention include Angelicae gigas Nakai, Angelica acutiloba Kitagawa and Angelica sinensis 25 Diels. The extract of the present invention may be prepared by any of the conventional methods using suitable solvents such as alcohols. For instance, a lower alcohol such as methanol and ethanol, preferably, 80 % methanol, is added to 30 the root of a plant of genus Angelicae and the mixture is allowed to stand at a temperature ranging from 15 to 80 0 C, preferably, 30 to 55 0 C, for a period ranging from 15 minutes to 48 hours, preferably, 30 minutes to 12 hours to obtain an extract. The resulting extract comprises ferulic acid and 35 decursinol in amounts ranging from 0.01 to 0.9 % by weight and 0.1 to 10 % by weight, respectively, based on the total WO 00/61131 PCT/KROO/00337 6 weight of the extract. Further, the extract may also be prepared by employing an organic solvent, e.g., acetone, chloroform and methylene chloride, and may be processed into a powder by drying under a reduced pressure. 5 The hydroxycinnamic acid derivative of formula I, decursinol or an extract of a plant of genus Angelicae containing same exerts a preventive or treating effect on dementia in a mouse Alzheimer's disease model: Administration of the inventive composition is effective in 10 preventing or treating memory impairment of a mouse induced by injecting which is established by administering 1 amyloid(1-42) directly into the cerebral ventricle of the mouse. The results of immunohistochemical staining to examine 15 histological changes induced by injecting $-amyloid(1-42) into the cerebral ventricle of a control mouse show that OX 42, a marker of microglia, increases temporarily in the cerebral cortex and then returns to a normal state. Further, it is also observed that the level of choline 20 acetyltransferase(ChAT), an enzyme synthesizing acetylcholine, decreases when P-amyloid(1-42) is administered. In contrast, for a mouse which has been previously administered with the hydroxycinnamic acid derivative of 25 formula I, decursinol or an extract of a plant of genus Angelicae before the administration of P-amyloid(1-42), the OX-42 level is much lower as compared with the control. Further, the decrease in the ChAT concentration observed with the control is not detected in the mouse administered 30 with the inventive composition. Thus, the hydroxycinnamic acid derivative of formula I, decursinol or an extract of a plant of genus Angelicae prevents or treats dementia through the protection of brain tissues by suppressing the activity of microglia which plays 35 an important role in the induction of neurotoxicity by P amyloid(1-42) and by preventing reduction of ChAT by P- WO 00/61131 PCT/KROO/00337 7 amyloid(1-42). Moreover, in spite of their potent efficacies, the hydroxycinnamic acid derivative of formula I, decursinol and an extract of a plant of genus Angelicae show little 5 toxicity in toxicity tests using rats and exert no adverse effects on the liver function. A pharmaceutical composition for preventing or treating dementia can be prepared by mixing the hydroxycinnamic acid derivative of formula I, decursinol or 10 an extract of a plant of genus Angelicae with a pharmaceutically acceptable excipient or carrier, or by diluting it with a pharmaceutically acceptable diluent in accordance with any of the conventional procedures. Examples of suitable carriers, excipients, and diluents are 15 lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starches, gum acacia, alginates, gelatin, calcium phosphate, calcium silicate, cellulose, methylcellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxy-benzoates, 20 propylhydroxybenzoates, talc, magnesium stearate and mineral oil. The formulations may additionally include fillers, anti-agglutinating agents, lubricating agents, wetting agents, flavors, emulsifiers, preservatives and the like. The compositions of the present invention may be formulated 25 so as to provide quick, sustained or delayed release of the active ingredient after their administration to a mammal by employing any of the procedures well known in the art. Thus, the formulations may be in the form of a tablet, pill, powder, sachet, elixir, suspension, emulsion, solution, 30 syrup, aerosol, soft and hard gelatin capsules, sterile injectable solution, sterile packaged powder and the like. The pharmaceutical composition of the present invention can be administered via various routes including oral, transdermal, subcutaneous, intravenous and 35 intramuscular introduction. Typical daily doses of the hydroxycinnamic acid derivative of formula I, decursinol and WO 00/61131 PCT/KROO/00337 8 an extract of a plant of genus Angelicae may range from about 0.5 to 50 mg/kg body weight, 0.3 to 30 mg/kg body weight and 5 to 500 mg/kg body weight, respectively, and they can be administered in a single dose or in divided 5 doses. However, it should be understood that the amount of the active ingredient actually administered ought to be determined in light of various relevant factors including the chosen route of administration, the age, sex and body weight of the individual patient, and the severity of the 10 patient's symptom; and, therefore, the above dose should not be intended to limit the scope of the invention in any way. On the other hand, the hydroxycinnamic acid derivative of formula I, decursinol or an extract of a plant of genus Angelicae can be incorporated in foods, as an additive or a 15 dietary supplement, for the purpose of preventing or treating dementia. Accordingly, the present invention also provides a food composition effective for preventing or treating dementia comprising an effective amount of the hydroxycinnamic acid derivative of formula I, decursinol or 20 an extract of a plant of genus Angelicae containing same. The foods may include various foodstuffs; beverages; gums; teas; vitamin complexes; and health foods. In order to prepare the foods having preventive or treating activity on dementia, the hydroxycinnamic acid 25 derivative of formula I, decursinol or an extract of a plant of genus Angelicae may be admixed with the raw materials during the preparation of foods or added to cooked foods. In this case, the content of the hydroxycinnamic acid derivative of formula I, decursinol and an extract of a 30 plant of genus Angelicae in a food may range from 0.05 to 10 % by weight, 0.05 to 10 % by weight and 1 to 40 % by weight, respectively. The following Examples are intended to further illustrate the present invention without limiting its scope. 35 Further, percentages given below for solid in solid mixture, liquid in liquid, and solid in liquid are on a WO 00/61131 PCT/KR0O/00337 9 wt/wt, vol/vol and wt/vol basis, respectively, and all the reactions were carried out at room temperature, unless specifically indicated otherwise. 5 Reference Example 1: Injection into Cerebral Ventricle The administration of -amyloid(1-42) to a mouse was carried out in accordance with the method described by Laursen & Belknap(J. Pharmacol. Methods, 16, 355-357(1986)). 10 Specifically, 5 Ll of phosphate-buffered saline containing 1.85 pg of P-amyloid(1-42) was put in a 50 Ll Hamilton syringe fitted with a 26 gauge needle, the tip of the needle was inserted into the bregma of the mouse and then the 1 amyloid(1-42) solution was administered thereto. Each mouse 15 of a control group received an equal amount of P-amyloid(42 1) in place of P-amyloid(1-42) . A passive avoidance test was carried out at days 1-2(day 1: training, day 2: test) and a Y-maze test, at days 3-4(day 3: training, day 4: test) after the administration. 20 Reference Example 2: Passive Avoidance Test In order to examine the learning and memory-retention ability of a mouse, a passive avoidance test was carried out 25 in accordance with the method described in Song et al., J. Neurochem., 71, 875-878(1998), as follows. A passive avoidance case equipped with a light room and a dark room was prepared, the floor of the dark room being designed to deliver an electrical shock to a test 30 animal. First, a mouse was put in the light room and, upon entering the dark room, it received an electrical shock at 0.25 mA for 1 sec. Twenty-four hours after the training, the mouse was put in the light room again and the time it took to enter the dark room was measured as a passive avoidance 35 time. The maximum time was set at 300 sec., i.e., in case when the mouse took more than 300 sec. to enter the dark WO 00/61131 PCT/KR00/00337 10 room, the passive avoidance time was determined to be 300 sec. Reference Example 3: Y-maze Test 5 Spontaneous alternation behavior of a mouse was examined by a Y-maze test in accordance with the method described in Starter et al., Psychopharmacology, 94, 491 495(1988) as follows. 10 The Y-maze consisted of three arms shaped like Y. A test mouse was placed in one of the arms such that it faced the arm's terminal and allowed to roan freely through the three arms for 8 hours. The number of alternation was determined by counting the number of occasions the mouse 15 passed the three arms consecutively. Spontaneous alternation behavior was determined as the percentage of the alternation number based on the total number of arm entries. Example 1: Preparation of an extract of a plant of genus 20 Angelicae 2 L of 80 % methanol was added to 1 kg of chopped root of Angelicae gigas Nakai and the mixture was heated at 40 0 C for 2 hours to obtain an extract. The extraction procedure 25 was repeated twice. The extract solution were combined, and methanol and moisture was evaporated therefrom by employing a reduced-pressure reflux condenser. Then, the resulting extract was dried thoroughly at a reduced pressure to obtain 290 g of the extract of Angelicae gigas Nakai. HPLC analyses 30 revealed that the extract contained decursinol and ferulic acid in amounts of 0.5 wt% and 0.07 wt%, respectively(Figs. 1A and 1B), the HPLC analyses being carried out under the following conditions: Decursinol 35 Column: Si60 (7 pm, 250 mm x 4 mm); Solvent: n hexane:EtoAc=1:1; Flow rate: 1.0 ml/min.; Detector: UV WO 00/61131 PCT/KROO/00337 11 340 nm Ferulic acid Column: RP-18(7 pLm, 250 mm x 4 mm); Solvent: 5 MeOH:water=l:3.5; Flow rate: 1.0 ml/min.; Detector: UV 258 nm. The above procedure was repeated to obtain extracts from Angelica acutiloba Kitagawa and Angelica sinensis Diels 10 and it was confirmed by HPLC analysis that the resulting extracts also contained ferulic acid and decursinol. Example 2: Effect of the Extract of Angelicae gigas Nakai on the Prevention of Dementia 15 Forty 4- to 5- week old mice each weighing 20 to 25 g were divided into four groups of equal number. The Angelicae gigas Nakai extract prepared in Example 1 was dissolved in water to concentrations of 0.08 %(w/v) and 0.1 %(w/v), 20 respectively, and the mice of two groups were provided with the resulting solutions instead of water for 4 weeks at a daily dose of 8 ml of the solution/mouse. The mice of the other two groups were provided with normal drinking water for 4 weeks. Thereafter, the mice of one of the two normal 25 drinking water groups were administered into their cerebral ventricle with 1.85 ptg of P-amyloid(42-1) ("control group") and the mice of the remaining three groups, with P amyloid(1-42) (Apl- 42 ), as in Reference Example 1. Then, a passive avoidance test was carried out for each group of 30 mice as in Reference Example 2 and the data attained were averaged for each group. As shown in Fig. 2A, the passive avoidance response time was significantly lower for the group administered with P-amyloid(1-42) only, as compared with the control group. 35 However, much improved passive avoidance response times were observed with the groups administered with 0.08 %(w/v) and WO 00/61131 PCT/KROO/00337 12 0.1 %(w/v) of the Angelicae gigas Nakai extract, respectively, as compared with the p-amyloid(1-42) group. The same procedure as above was repeated by varying the administration period of 0.1 % (w/v) of the Angelicae 5 gigas Nakai extract from 1 to 2 to 4 weeks. The result in Fig. 2B shows that improvement in the passive avoidance response time becomes evident when the administration of the Angelicae gigas Nakai extract is continued for 2 weeks or longer. 10 Example 3: Effect of Ferulic Acid on Prevention of Dementia The effect of ferulic acid, a component of the Angelicae gigas Nakai extract, on the prevention of dementia 15 was examined as follows. Fifty 4- to 5-week old mice each weighing 20 to 25 g were divided into five groups by equal number. Ferulic acid was dissolved in water to concentrations of 0.002 %(w/v), 0.004 %(w/v) and 0.006 %(w/v), respectively, and the mice of 20 three groups were provided with the resulting solutions instead of water for 4 weeks at a daily dose of 8 ml of the solution/mouse. The mice of the other two groups were provided with normal drinking water for 4 weeks. Thereafter, the mice of one of two normal drinking water groups were 25 administered into their cerebral ventricle with 1.85 pg of P-amyloid(42-1) ("control group") and the mice of the remaining four groups, with -amyloid(1-42) (A 42 ) , as in Reference Example 1. Then, a passive avoidance test was carried out for each group of mice as in Reference Example 2 30 and the data attained were averaged for each group. As shown in Fig. 3A, the passive avoidance response time was significantly lower for the group administered with -amyloid(1-42) only, as compared with the control group. However, the decrease in the passive avoidance response time 35 of the groups preventively administered with ferulic acid for 4 weeks was prevented dose-dependently.

WO 00/61131 PCT/KROO/00337 13 Meanwhile, the above procedure was repeated by varying the period of administration of 0.006 %(w/v) of ferulic acid among 1, 2, 3 and 4 weeks. The result in Fig. 3B shows that the passive avoidance response time becomes increasingly 5 higher with the period of administration. Further, Y-maze tests were carried out employing the above-prepared mice as in Reference Example 3. The result in Fig. 4A shows that, as compared with the group administered with f-amyloid(1-42) only, the alternation 10 behavior(%) of the groups administered with ferulic acid was higher and increased in proportion to the period of administration. However, as shown in Fig. 4B, the number of arm entries, which represents a measure of spontaneous movement, is nearly the same for all groups. This result 15 demonstrates that ferulic acid exerts therapeutic influence on the memory, rather than on movement. Passive avoidance tests were also conducted as above using mice administered with 0.006 %(w/v) of ferulic acid or isoferulic acid for 4 weeks. The result in Fig. 5 shows that 20 the passive avoidance response time observed for the isoferulic acid group was similar to that of the ferulic acid group, demonstrating that isoferulic acid is as effective as ferulic acid in preventing dementia. 25 Example 4: Effect of Decursinol on Prevention of Dementia The effect of decursinol, a component of the Angelicae gigas Nakai extract, on the prevention of dementia was examined as follows. 30 Forty 4- to 5-week old mice each weighing 20 to 25 g were divided into four groups of equal number. Decursinol was dissolved in corn oil, mixed with a mouse fodder, and the mice of two groups were provided with the resulting fodder for 4 weeks at a daily dose of 7.5 mg decursinol/kg 35 or 15 mg decursinol/kg. The mice of the other two groups were provided with a normal mouse fodder containing an equal WO 00/61131 PCT/KROO/00337 14 amount of corn oil as above for 4 weeks. Thereafter, the mice of one of the two normal fodder groups were administered, into their cerebral ventricle, with 1.85 pg of P-amyloid(42-1) ("control group") and the mice of the 5 remaining three groups, with P-amyloid(1-42) (Ap3 1 2 ) , as in Reference Example 1. Then, a passive avoidance test and a Y maze test were carried out for each group of mice as in Reference Examples 2 and 3, respectively, and the data attained were averaged for each group. 10 As shown in Fig. 6A, the decrease in the passive avoidance response time due to the administration of P amyloid(1-42) was prevented in the groups preventively administered with decursinol. Figs. 6B and 6C show that, as compared with the group 15 administered with j-amyloid(1-42) only, the alternation behavior(%) of the groups administered with decursinol was higher and increased dose-dependently. However, the number of arm entries, which represents a measure of spontaneous movement, is nearly the same for all groups. These results 20 demonstrate that decursinol exerts therapeutic influence on the memory, rather than on movement. In order to confirm the synergism between ferulic acid and decursinol, a passive avoidance test was carried out as in Reference Example 2 using mice administered with 25 0.002 %(w/v) of ferulic acid, 2 mg/kg of decursinol or a mixture thereof as above. Further, a passive avoidance test was also carried out using mice administered with 0.003 %(w/v) of ferulic acid, 3 mg/kg of decursinol or a mixture thereof. In the two experiments, a group of mice 30 administered with 0.006 %(w/v) of ferulic acid was employed as a comparative group. The results in Figs. 7A and 7B show that a mixture of ferulic acid and decursinol, each of them being in a low amount having no dementia-preventive effect, exhibit a 35 significant preventive effect. This result demonstrates the synergism between ferulic acid and decursinol.

WO 00/61131 PCT/KROO/00337 15 Example 5: Examination of the Activity of Ferulic Acid Protecting Brain Cells (1) Immunohistochemical staining of OX-42 at one day after 5 the administration of -amyloid 4- to 5-week old mice each weighing 20 to 25 g was divided into three groups. Ferulic acid was dissolved in water to a concentration of 0.006 %(w/v), and the mice of 10 one group were provided with the resulting solution instead of water for 4 weeks. The mice of other two groups were provided with normal drinking water for 4 weeks. Thereafter, the mice of one of two normal drinking water groups were administered, into their cerebral ventricle, with 1.85 pg of 15 P-amyloid(42-1) ("control group") and the mice of the remaining two groups, with f-amyloid(1-42) (Al 42 ), as in Reference Example 1 One day after the administration of P-amyloid, each of the mice was anesthetized with sodium pentobarbital and its 20 abdomen was incised. The mouse was fixed by passing 4% paraformaldehyde through its left ventricle and its brain was excised. In accordance with the method described in Cho et al., J. Comp. Neurol., 369: 264-276(1996), a section was prepared 25 from the excised brain and immunohistochemical staining was carried out in order to stain OX-2 in the pyriform cortex and the amygdaloid nucleus by employing 1:500 dilution of anti-OX-42 antibody(Halan(Sera-Lab)). Then, the section was observed with a microscope at magnifications of 200 and 400, 30 respectively. The result is shown in Figs. 8a to 8f, wherein Figs. 8a to 8c were taken at a magnification of 200, and Figs. 8d to 8f, at a magnification of 400. As compared with the control group(Figs. 8a and 8d), increased OX-42 was observed with 35 the group administered with P-amyloid(1-42) only(Figs. 8b and 8e), while OX-42 is much less pronounced with the group WO 00/61131 PCT/KRO0/00337 16 administered with ferulic acid followed by -amyloid(1 42) (Figs. 8c and 8f). (2) Immunohistochemical staining of ChAT 5 days after the 5 administration of P-amyloid Three groups of mice were administered with ferulic acid and/or P-amyloid in accordance with the method of (1). 5 days after the administration of P-amyloid, 10 immunohistochemical staining was carried out according to the method of (1) except for employing 1:750 dilution of anti-choline-acetyltransferase (ChAT) antibody(Chemicon) in order to stain ChAT, an enzyme for acetylcholine synthesis, in the septal nucleus wherein acetylcholine neurons are 15 distributed. The result is shown in Figs. 9a to 9c. As compared with the control group(Fig. 9a), decreased ChAT was observed with the group administered with P-amyloid(1-42) only(Fig. 9b) while the decrease was suppressed in the group administered 20 with ferulic acid followed by f-amyloid(1-42) (Fig. 9c). Example 6: Effect of ferulic acid in inhibiting the damage of neurons 25 In accordance with the method of Wie et al. (Neurosci. Lett., 225: 93-96(1997)), glia was cultured from cells of the cerebral cortex of a mouse and neurons of mouse cerebrum were cultured by employing the glia as a substrate. The culture of mouse cerebral neurons was divided into 30 three groups. Neurons of one group received no treatment(control group). Neurons of the other two groups were treated with 25 p1M of p-amyloid(1-42), and one of these two groups were treated with 100 p.M of ferulic acid 30 minutes before the administration of P-amyloid(1-42). 35 The degree of damage in neurons was determined by measuring the concentration of lactate dehydrogenase(LDH), WO 00/61131 PCT/KROO/00337 17 which was released from the damaged or disrupted neurons into the culture medium, in accordance with the method of Wie et al. Samples of the culture medium were taken at 24 and 48 hours after the administration of f-amyloid(1-42), 5 respectively, and their LDH concentrations were measured with a microplate reader. As shown in Fig. 10, as compared with the control group, the LDH concentration is significantly higher for the group administered with P-amyloid(1-42), while a much lower LDH 10 concentration was observed with the group administered with ferulic acid followed by -amyloid(1-42) . This result demonstrates that ferulic acid inhibits the damage of neurons caused by P-amyloid(1-42). 15 Example 7: Toxicity of the Extract of Angelica gigas Nakai Forty(20 males and 20 females) 4 week-old Sprague Dawley rats were bred for a week under a condition of temperature 22

±

3 "C, relative humidity 50 ±10% and intensity 20 of illumination 150-300 Lux. The rats were divided into four groups each consisting of 5 males and 5 females. The extract of Angelica gigas Nakai prepared in Example 1 was dissolved in corn oil and administered orally to the rats of four groups at doses of 300, 1,000, 3000 and 25 10,000 mg/kg, respectively. The extract was administered once and the rats were observed for 7 days for signs of adverse effect or death. Further, on the 7th day, the rats were sacrificed and the internal organs were visually examined. The weight changes of the rats were recorded every 30 day to examine the effect of the extract of Angelica gigas Nakai. The result showed that LD 50 of the extract of Angelica gigas Nakai is 3,722 mg/kg for males and 2,804 mg/kg for females. The autopsy showed that the rats did not develop 35 any pathological abnormality at a dose of 1,000 mg/kg or less. Further, no weight loss was observed during the 7-day WO 00/61131 PCT/KROO/00337 18 test period in case of the rats administered with the extract at a dose of 1,000 mg/kg or less. Formulation Example 5 100 mg of the Angelicae gigas Nakai extract prepared in Example 1, 45 mg of milk calcium, 122 mg of microcrystalline cellulose, 15 mg of isoflavon, 2.5 mg of ginkgo extract, 2 mg of Zizyphus jujuba extract, 0.25 mg of 10 vitamin B 1 , 0.3 mg of vitamin B 2 , 0.0025 mg of vitamin D 3 and 2.5 mg of magnesium stearate were mixed thoroughly and filled into a hard gelatin capsule to prepare a hard gelatin capsule formulation. 15 While the invention has been described with respect to the above specific embodiments, it should be recognized that various modifications and changes may be made to the invention by those skilled in the art which also fall within the scope of the invention as defined by the appended claims.

Claims (14)

1. A composition for preventing or treating dementia comprising a hydroxycinnamic acid derivative of formula I or 5 a pharmaceutically acceptable salt thereof: R(2 10 OR OH wherein, R1 is H or CH 3 , H \ -OH 15 R2 is -CH=CHCOOH or -CH=CHCOO-C C I I \OH C C C HO COOH

2. The composition of claim 1, wherein the 20 hydroxycinnamic acid derivative of formula I is ferulic acid or isoferulic acid.

3. The composition of claim 1, which further comprises decursinol. 25

4. A composition for preventing or treating dementia comprising decursinol or a pharmaceutically acceptable salt thereof. 30

5. A composition for preventing or treating dementia comprising an extract of a plant of genus Angelicae containing the hydroxycinnamic acid derivative of formula I or decursinol. 35

6. The composition of claim 5 wherein the extract is prepared by extracting the root of a plant of genus WO 00/61131 PCT/KROO/00337 20 Angelicae with a lower alcohol.

7. The composition of claim 5 or 6 wherein the plant of genus Angelicae is selected from the group consisting of 5 Angelicae gigas Nakai, Angelica acutiloba Kitagawa and Angelica sinensis Diels.

8. A food composition for preventing or treating dementia comprising a hydroxycinnamic acid derivative of formula I or 10 a pharmaceutically acceptable salt thereof: R(2 15 OR OH wherein, R' is H or CH 3 , HX OH 20 R 2 is -CH=CHCOOH or CHCHCOOC c H * C C HO \ COOH

9. The food composition of claim 8, wherein the 25 hydroxycinnamic acid derivative of formula I is ferulic acid or isoferulic acid.

10. The food composition of claim 8, which further comprises decursinol. 30

11. A food composition for preventing or treating dementia comprising decursinol or a pharmaceutically acceptable salt thereof. 35

12. A food composition for preventing or treating dementia comprising an extract of a plant of genus Angelicae WO 00/61131 PCT/KROO/00337 21 containing the hydroxycinnamic acid derivative of formula I or decursinol.

13. The composition of claim 12 wherein the extract is 5 prepared by extracting the root of a plant of genus Angelicae with a lower alcohol.

14. The composition of claim 12 or 13 wherein the plant of genus Angelicae is selected from the group consisting of 10 Angelicae gigas Nakai, Angelica acutiloba Kitagawa and Angelica sinensis Diels.